Taiwan FDA registration d01d977aee57328035a6a7370d5c241a
"Medtronic" Isos Therapy Controller
TW: “美敦力”艾瑟斯治療控制器
Taiwan·Risk Class 3·MEDTRONIC NEUROMODULATION·Registered Apr 19, 2007 – Apr 19, 2017CancelledRegistration details
- Analysis ID
- d01d977aee57328035a6a7370d5c241a
- Customs Code
- DHA00601802700
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5840 Implantable intracranial/subdermal stimulator for pain relief
- Import Information
- import
Dates and status
- Registration Date
- Apr 19, 2007
- Expiry Date
- Apr 19, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" Isos Therapy Controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d01d977aee57328035a6a7370d5c241a and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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